Earnings call transcript: GeneDx Q2 2025 beats forecasts, stock surges

GeneDx Holdings Corp reported a strong financial performance for the second quarter of 2025, significantly surpassing earnings and revenue forecasts. The company reported earnings per share (EPS) of $0.50, well above the anticipated $0.12, marking a surprise of 316.67%. Revenue reached $102.7 million, exceeding the forecasted $85.45 million by 20.19%. This positive earnings report led to a pre-market stock surge of 24.36%, with shares reaching $105.59. According to InvestingPro data, the company has demonstrated remarkable momentum with a 152% return over the past year, though it currently trades above its Fair Value estimate.

Key Takeaways

• GeneDx posted a 49% year-over-year increase in Q2 2025 revenues.
• The company achieved a record adjusted gross margin of 71%.
• Exome and genome revenues grew by 69% year-over-year.
• GeneDx’s stock surged over 24% pre-market following the earnings release.
• Full-year revenue guidance was set between $400 million and $415 million.

Company Performance

GeneDx demonstrated robust growth in the second quarter, highlighted by a 49% year-over-year increase in revenues. The company continues to lead in the rare disease genetic testing market, with a focus on expanding its pediatric and NICU testing capabilities. GeneDx’s strategic initiatives, including the integration of Fabric Genomics and the launch of new indications, have positioned the company for sustained growth. InvestingPro analysis reveals the company maintains a healthy financial position with a current ratio of 3.25, indicating strong liquidity to support its expansion plans. For deeper insights into GeneDx’s growth potential and comprehensive analysis, investors can access the detailed Pro Research Report, available exclusively to InvestingPro subscribers.

Financial Highlights

• Revenue: $102.7 million, up 49% year-over-year.
• Earnings per share: $0.50, significantly exceeding the $0.12 forecast.
• Adjusted gross margin: 71%, a record high for the company.
• Adjusted net income: $15 million, marking the fourth consecutive quarter of profitability.
• Cash and equivalents: $135.5 million.

Earnings vs. Forecast

GeneDx’s EPS of $0.50 outperformed the forecast of $0.12, resulting in a substantial surprise of 316.67%. Revenue also surpassed expectations, reaching $102.7 million compared to the forecasted $85.45 million, a 20.19% surprise. This marks a significant improvement over previous quarters, showcasing the company’s strong operational execution.

Market Reaction

Following the earnings announcement, GeneDx’s stock experienced a notable pre-market increase of 24.36%, with shares trading at $105.59. This surge reflects investor confidence in the company’s ability to exceed expectations and deliver strong financial results. The stock’s performance is a testament to GeneDx’s market leadership and growth potential. InvestingPro indicates the stock has been quite volatile, with a beta of 2.08, while analyst targets range from $78 to $115 per share. The company’s overall financial health score is rated as "GOOD" by InvestingPro’s comprehensive evaluation system, which considers multiple financial metrics and growth indicators.

Outlook & Guidance

GeneDx has provided full-year revenue guidance of $400 million to $415 million, with exome and genome revenue expected to range between $345 million and $355 million. The company anticipates 30%+ volume growth in 2025 and aims to expand its presence in the pediatric market by 2026. GeneDx remains focused on NICU and new indication growth as key drivers of future performance.

Executive Commentary

CEO Kathryn Stuhlen emphasized the company’s leadership in rare disease diagnosis, stating, "We diagnose more rare diseases than anyone in the world." She also highlighted GeneDx’s vision for early genetic information delivery: "Our vision is for a world where genetic information is delivered as early as possible." Stuhlen underscored the company’s proactive approach to healthcare, saying, "We’re shifting health care from reactive to proactive."

Risks and Challenges

• Potential Medicaid billing challenges could impact revenue cycles.
• Market saturation in the rare disease genetic testing sector may limit growth.
• Macroeconomic pressures could affect healthcare spending and reimbursement rates.
• Integration risks associated with recent acquisitions, such as Fabric Genomics.
• Regulatory changes impacting genetic testing practices and reimbursement.

Q&A

During the earnings call, analysts inquired about the company’s strategy for improving reimbursement rates and entering the pediatrician market. GeneDx addressed these concerns by detailing its enhanced revenue cycle management and efforts to engage 25,000 pediatricians for future market expansion. Additionally, the company discussed the implementation of NICU testing and the potential challenges associated with Medicaid billing.

Full transcript - GeneDx Holdings Corp (WGS) Q2 2025:

Conference Operator: Day and thank you for standing by. Welcome to the GeneDx Second Quarter twenty twenty five Earnings Conference Call. At this time, all participants are in a listen only mode. After the speakers’ presentation, there will be a question and answer session. To ask a question during the session, you’ll need to press 11 on your telephone.

You will then hear an automated message advising your hand is raised. To withdraw your question, please press 11 again. Please be advised that today’s conference is being recorded. I would now like to turn the conference over to Sabrina Dunbar, Investor Relations. Please go ahead.

Sabrina Dunbar, Investor Relations, GeneDx: Thank you, operator, and thank you to everyone for joining us today. On the call, we have Kathryn Stuhlen, President and Chief Executive Officer and Kevin Feeley, Chief Financial Officer. Earlier today, GeneDx released financial results for the second quarter ended 06/30/2025. Before we begin, please take note of our cautionary statements. We may make forward looking statements on today’s call, including about our business plans, updated 2025 guidance, and outlook.

Forward looking statements inherently involve risks and uncertainties and only reflect our view as of today, July 29, and we are under no obligation to update. When discussing our results, we refer to non GAAP measures, which exclude certain items from reported results. Please refer to our second quarter twenty twenty five earnings release and slides available at ir.genevx.com for definitions and reconciliations of non GAAP measures and additional information regarding our results, including a discussion of factors that could cause actual results to materially differ from forward looking statements. And with that, I’ll turn the call over to Kathryn.

Kathryn Stuhlen, President and Chief Executive Officer, GeneDx: Thanks, Sabrina, and good morning, everyone. Today, I’m incredibly proud to share that our team’s work not only met but exceeded expectations, achieving a major milestone of delivering over $100,000,000 in revenue in a single quarter for the first time. Our strong second quarter performance was driven by our core business, underscoring its strength and resilience. These results, coupled with the ever expanding opportunities ahead, demonstrate that we’re just beginning to deliver on the promise of how our genomic technology can fundamentally transform health care. Our vision is for a world where genetic information is delivered as early as possible to prevent unnecessary suffering and lead to healthier lives for all.

Today, we’re waiting for symptoms to develop and for disease to progress, not only over the course of months, but over the course of years. We’ve never been more resolute about our commitment to radically change this. Shifting from sick care to health care, driving better health outcomes, better economic value, and a better health care system for us all. At a recent all company meeting, a patient advocate reminded us why we do this. His diagnostic odyssey lasted nearly two decades before he received answers.

His story highlights a systemic issue. Care often starts too late, with children waiting an average of five years for a genetic diagnosis. This is totally unacceptable given the solutions we have in hand today at GeneDx. Thanks to our investment in innovation and scale, genomic testing, once considered slow and costly, now delivers answers not in weeks or even days, but sometimes hours, and at costs lower than ever before. Our technology is shifting health care from reactive to proactive, benefiting both patients and the health care system.

GeneDx is uniquely positioned to bring genomic information into mainstream medicine. We diagnose more rare diseases than anyone in the world and are the number one genetic testing brand amongst pediatric health care providers with 80% market share amongst geneticists. Our unmatched expertise and proprietary data set enriched for rare disease, inclusive of asymptomatic individuals, supported by clinical data, and representative of The US population has enabled us to identify over 500 gene disease relationships to date, ensuring more patients receive answers with greater accuracy. This is what sets GeneDx apart and why we’re the clear leader in ushering in the next era of genomics informed health care. Our competitive advantage grows with every patient we test.

With over 850,000 exomes and genomes and over 7,000,000 phenotypic data points, we’ve built one of the world’s most comprehensive genomic data sets, and we are putting it to work for patients. Our proprietary interpretation platform grows stronger with each new patient we test, building upon our data advantage and leveraging AI to drive greater accuracy, speed, and scalability. Our lead will only continue to expand as we integrate Fabric Genomics and its proprietary algorithms into the core platform, further strengthening our competitive edge and positioning us for unprecedented scale. As we grow the business and reach new clinicians, we will continue to stand out on quality, accuracy, scale, and experience. Put another way, there’s no one who can check all the boxes of being better, faster, and cheaper than GeneDx.

We have everything we need to remain the leader even as competition emerges. We’ve established a strong foothold with geneticists who choose us eight times out of 10, demonstrating the trust we’ve built in our core market. These geneticists are key influencers, and their continued support is helping us win over other specialists as we grow. And that’s what’s happening today as our reach has broadened and deepened. In the second quarter, pediatric neurologists made up a majority of new exome and genome ordering providers, and we’ve now captured nearly a third of our target clinicians in this segment.

Most of our Q2 volume growth came from patients within our core indications, but we’re also seeing early signs of increased adoption as we introduce new indications like cerebral palsy. This expansion has helped us reach fourteen percent of our target patients, which is growth from last quarter as it represents the same share of a larger patient pool. In Q2, we also began engaging pediatric immunologists, an entirely new audience, focusing on children with inborn errors of immunity. Based on our experience with pediatric neurologists, we expect to see momentum build in these new indications and call points as our relationships deepen. Another growth driver for the second half is the NICU, which represents a billion dollar opportunity.

Fewer than five percent of babies in the NICU currently receive a genetic test, so this is an important market for us to develop. Each year, two hundred and thirty five thousand infants are treated at approximately 800 level three or level four NICUs that could benefit from rapid genomic testing, twenty percent of which are already GeneDx clients. Importantly, 42 out of 50 top NICUs have already ordered testing from us this year, and we’re continuing to take a top down and bottom up approach to scale volume. We recognize the need for three things to succeed in the NICU, data, product, and scale, and we now have all three. Our enterprise sales team is equipped with SeekFirst data demonstrating up to sixty percent of infants in high acuity NICUs would benefit from rapid genome sequencing and a CFO calculator that demonstrates the financial benefits testing to each hospital.

Our ultra rapid test delivers results in as early as forty eight hours, and Epic Aura integrations are supporting a seamless delivery of our testing to patients. We have three health systems live on Epic Aura, and we expect to have a dozen hospitals on board and a few thousand tests performed by year end. As protocols evolve and whole system engagement increases, we’re well positioned to scale NICU testing significantly. While the NICU represents a significant and growing frontier for us, an even larger transformative opportunity is the general pediatrics market. This shift is largely driven by recent guidance from the American Academy of Pediatrics recommending pediatricians use exome and genome sequencing as a first tier test for children with global developmental delay or intellectual disability.

This is a sea change in pediatric health care. Previously, pediatricians referred these children to specialists beginning a long, painful odyssey for families. Now, with new guidance, that can all change. The general pediatrician market remains untapped. Of the 60 thousand general pediatricians in The US, about twenty five thousand diagnosed children with developmental or intellectual delays, representing six hundred thousand children who could benefit from our testing.

To accelerate adoption of the new guidelines, we will have a presence at the annual AAP meeting in September, where we’ll engage directly with clinicians. We’re also investing in continuing medical education to ensure pediatricians understand the need guidance and how to integrate exome and genome testing into their practice. By collaborating with local AAP chapters and leveraging our marketing engine, we’re building awareness and trust in GeneDx, making it easier for pediatricians to navigate this shift and confidently order our tests. Concurrently, we’re improving our customer experience to make it more accessible to a non specialist. We’re taking a targeted commercial approach in Q3, starting with the fewer than five percent of pediatricians already ordering genetic tests for a high number of CDID patients, allowing us to learn and refine our strategy before scaling up.

With a $2,500,000,000 market opportunity ahead, we expect the broader adoption to take eighteen to twenty four months. While pediatricians represent a significant long term opportunity, for the remainder of the year, we expect growth to be driven by our core customer base of specialists diagnosing patients with epilepsy, autism, and DDID, supplemented by new indications and the NICU. Our work to date has shown the value of testing symptomatic patients, but we know the next step forward is to provide a diagnosis before symptoms begin with genomic newborn screening. The Guardian study has shown that whole genome sequencing can identify serious treatable genetic conditions in over three percent of newborns, ninety two percent of which would have been missed by standard screening. Legislative progress, such as Florida’s Sunshine Genetic Act, is paving the way for broader adoption.

With experience screening over 17,000 newborns, our robust underlying data, and our ability to deliver at scale, we are uniquely positioned to play a key role as this initiative evolves. All the while, our team is forging partnerships with pharmaceutical companies of every size, because while only five percent of rare diseases have an approved therapy, we know that our unparalleled genomic data can help accelerate the development of new treatments. We are positioned as a partner of choice, ready to support biopharma and harnessing genetic insights to inform and transform therapeutic pipeline. Our commitment is simple: Get families the answer they need sooner, helping patients get on the right path to better health while reducing unnecessary costs across the health care system. Not only are we leaders in genomic testing, but we’re extending that lead and continually raising the bar by investing in our strategy, our technology, and our people.

While our mission is bigger than profitability, we’re proud that we’ve built a business that is both purposeful and profitable. That success is thanks to our dedicated team, our partners, and a shared belief in what’s possible when innovation meets conviction. With that, I’ll hand things over to Kevin.

Kevin Feeley, Chief Financial Officer, GeneDx: Thanks, Katherine, and thank you all for joining us today. We reported second quarter twenty twenty five revenues of $102,700,000 a 49% increase year over year. That total includes a record high of $85,900,000 in revenue from Exome and Genome, up 69% from the same quarter last year. The average reimbursement rate for Exome and Genome was over $3,700 a test in the quarter. That’s up from approximately $3,400 last quarter, and there’s nothing I would call out in the second quarter results as unique or one time.

We’re driving sustainable reimbursement rate improvements across both commercial and Medicaid payers by demonstrating the value necessary to expand policy. Our use of technology and process design are helping to avoid unnecessary nonmedical documentation and procedural denials. As I’ve often said, revenue cycle improvements aren’t always linear some periods outperform others. Q2 was one of those standout quarters, though, reinforcing our durable long term improvement trend. As we sit here today, business fundamentals have never been stronger, and our serviceable market continues to expand.

We remain on track to deliver our full year guide of at least 30% year over year volume growth. We reported twenty three thousand one hundred and two exome and genome tests in the 2025, up 28% compared to the second quarter of last year. The first half of the year has continued to play out as anticipated, providing conviction in the back half, and with several catalysts to come. This quarter, the majority of growth came from existing docs, and we are seeing strong early signals that new indications like cerebral palsy are driving increased same store sales. And importantly, our expansion into new indications makes GeneDx even more attractive to new account targets.

In the back half of this year and beyond, we’ll begin to layer on new growth curves from the NICU and from pediatric immunologists and other specialists, and from the pediatricians backed by AAP, and from newborn screening, and from international contribution, and of course, all of that is supplemented by the long term potential to establish a meaningful diversified revenue stream by putting the unparalleled nature of the GeneDx data to work for healthcare partners to accelerate drug discovery and development. Over the last ten years, we’ve moved from pioneering exome and genome to gaining the hard earned trust of the expert community, to developing the best in class product, to becoming the largest provider of rare disease diagnosis. All of this has established unique credibility for GeneDx to lead in all of these new markets. Now turning to gross margin. We again expanded total company adjusted gross margin to a record high of 71%, driven by all three of favorable mix shift, improved reimbursement, and lower COGS.

There is room to run-in terms of reducing COGS in the future by combining the best of capabilities between GNDX and Fabrik as we lean into the best possible algorithms to optimize dry lab processes. Adjusted operating expenses were $58,000,000 That is up in terms of aggregate dollars, representing investments in future growth in the addition of fabric. However, we are driving increased leverage. Total OpEx was 56% of revenue in the 2025 compared to 65% in the 2024. Our team has the experience necessary to properly balance innovation and growth with the skill to relentlessly look for efficiency, and we’ll do just that moving forward.

Where we see clear opportunities to invest to accelerate growth, to open new markets, and to take share, we will do so, all within an envelope of staying profitable. On the bottom line, we generated $15,000,000 in adjusted net income in the 2025. That’s our fourth consecutive quarter of profitability on that basis, having now cemented the business sustainably in the black. Our business has the bones for durable, high growth, all with the ability to drive EPS accretion over time. On the balance sheet, cash, cash equivalents, and marketable securities totaled $135,500,000 as of 06/30/2025.

As a reminder, the 2025 included a payment of $33,200,000 at closing to acquire Fabry. And now on to guidance. We’re raising our top line total revenue guidance to between 400,000,000 and $415,000,000 for full year 2025. We’re raising exome and genome revenue guidance to deliver between 4852% growth for the full year 2025. The math on that is exome and genome revenue of $345,000,000 to three fifty five million dollars We reaffirm our expectation to deliver at least 30% exome and genome volume growth for full year 2025.

We’re raising our expectation for full year adjusted gross margin to between 6871%, and we once again reaffirm our expectation to remain profitable each quarter for the full year of 2025 on an adjusted net income basis. With that, I’ll turn it back to Kathryn.

Kathryn Stuhlen, President and Chief Executive Officer, GeneDx: Thank you, Kevin, and thank you to our entire team for their continued dedication to the patients and families we serve. We believe the future of health care is about proactive, personalized care. That means understanding as early as possible whether a person has a genetic condition so that care can be tailored, risks can be managed, and outcomes improve. This is the future of medicine. This is the genome era, and we’re proud to be leading the way.

With that, we welcome your questions. Thank you.

Conference Operator: Our first question for the day will be coming from David Westenberg of Piper Sandler. Your line is open.

David Westenberg, Analyst, Piper Sandler: Thank you for taking the question. On such a great quarter. My first one here is for Kevin. ASPs trounced estimates by a lot. You kind of mentioned there’s no one time thing in the quarter, but it was a pretty big move.

So can you maybe go back a couple of quarters, assuming this is

Analyst: ebbs and flows, are there a

David Westenberg, Analyst, Piper Sandler: couple of discrete drivers to think about over the last four quarters, maybe like a few states that won that all covered all at the same time or anything to think about your benefits that maybe manifested this quarter that we could think about maybe comping or any other thing in kind of the go forward basis?

Kevin Feeley, Chief Financial Officer, GeneDx: Yeah. Thanks, Dave. I’d say you were to roll back the clock and go back towards the 2023, we made major overhauls to the team and processes across the revenue cycle to identify ways to more closely adhere to documentation requirements on a payer by payer basis, and that’s paid off handsomely. And so as it relates to reducing denials across commercial payers, it’s more so our continued ability to improve payment rates by reducing what I’ll call unnecessary documentation or procedural denials. That work has been ongoing for a year, and we continue to invest in finding ways to adhere to necessary requirements to get paid fairly for the work that we perform.

And of course, on the Medicaid population, a large portion of our business does run through Medicaid, state Medicaid programs, and there’s been a steady flow of new states picking up Medicaid coverage over the last year to two years. We’re now up to 35 states that cover exome and genome on an outpatient basis, which includes just two new ones this quarter that picked up coverage, and 17 that cover rapid genome on the inpatient side. So there’s no doubt that we’re benefiting from more and more state Medicaid coverage that’s, of course, volume that we’ve been serving well ahead of coverage. So it was always there in terms of volume, but not necessarily paid volume, and happy to see that pulling through. My comment on the second quarter is more so to say there’s nothing I would call out that’s leading to that higher rate of the second quarter as anything outside of us just continuing to collect better by reducing denials.

So no major appeal wins to call out, just the good hard work to ensure that we’re boosting collection rate by avoiding unnecessary denial.

David Westenberg, Analyst, Piper Sandler: Got it. Thank you very much. This is probably more for Kathryn. As you’re thinking about going after the pediatric market in 2026, can you talk about balancing an economically sound approach with going after this really big opportunity and how we should think about kind of the ramp in investment there? Maybe that’s a little bit of Kevin too, but anyway, thank you.

Kathryn Stuhlen, President and Chief Executive Officer, GeneDx: Yeah, that’s great. So, the general pediatric opportunity is, of course, a massive one, and it’s one that we have to build. And so, I think your question about how do we balance particularly the core of our business and growth in ped neuro, where we’ve been continuing to see great success versus building a market is really important. The runway on the ped neuro side of things continues to be a really critical opportunity for us. So, we’re gonna continue to put the vast majority of our focus, of course, there for the remainder of this year and into 2026 and ’twenty seven as well, as we start to build this broader general pediatrician market.

The first step for us beyond the guidelines being published really comes down to a number of things. So, one, our sales team will continue to focus on PEEP neuras, but we’ve got a very targeted approach to the pediatricians who are ordering testing from us today. So, we feel like we’ve got the right balance, keeping our eye on the ball for the near term opportunity. I would say second, we’ll be at AAP, which is in September, we’ll start to educate the general pediatricians at that meeting, and through local chapters, and through medical education. Our market access team is bringing the guidelines to all of the payers to ensure that the medical policy really gets updated to be in line with AAP guidelines.

And then we’ll continue to extend our marketing investment that we kicked off in June to raise awareness. So, we think that we’re taking a really prudent approach to the investment in the current market expansion in pedunos and other specialists, while we take on the future market on general pediatricians. I’d say the other piece that we have an eye on is how do we continue to make it easier for a non expert to order our testing? So, we’ve begun to invest earlier this year, in fact, already embedded in our plans for 2025 in simplifying the ordering experience, making it easier for a non expert to understand the results and the clinical action plan for the next step. So, our product and technology team has, I would say, really important roadmap that we need to realize to fully be able to take over that general pediatrician opportunity.

David Westenberg, Analyst, Piper Sandler: Thank you so much and congrats again.

Conference Operator: Thank you. One moment for the next question. And our next question will be coming from the line of Dan Brennan of TD Cowen. Your line is open.

Dan Brennan, Analyst, TD Cowen: Great, thank you and congrats obviously on a really strong quarter. Maybe could you speak a little to and Catherine and Kevin, you both touched on it during the prepared remarks, but just as we think about volumes, which were good in the quarter, you talked about the bridge to the second half. Just give us a little color on how the NICU is going, Kind of what’s how do we think about the impact in the back half of the year from the EMR integrations and as well from some of these newer indications? Just wondering how the early progress has been and kind of what we assume to kind of bridge to the 30% volume growth?

Kathryn Stuhlen, President and Chief Executive Officer, GeneDx: Awesome. So, starting with the outpatient opportunity, as we said, most of the volume that we saw in the second quarter came from our core meaning pediatric neurologist who had been ordering from us. About 25% of the volume growth came from new clinicians. And so, think what we saw in Q2 continued great growth in terms of the existing indications starting to be amplified by new indications as well. We kicked off cerebral palsy in March.

We started calling on pediatric immunologists in April. So, we expect that those are going to continue to really pick up. We saw some early indications that it amplified Q2, but we think Q3 and Q4 are going be when we start to see the additional benefit from new indications. So, as we think about the con scores of Q3 and Q4, we think volume growth will be bolstered by new indications in the second half of the year. On the NICU side of things, you know, that’s such an important new market for us.

And we’re really pleased with all of the progress that we’ve made. We have three health systems that are live with Epic, and we’re seeing volumes come through those three health systems. And we’ll have 12, at least 12 in the second half of the year. So, the sales team will really be focused, and this is the enterprise sales team, so different from the outpatient team. They’re focused now on pulling those volumes through once Epic sites are coming online.

So, we’ll see some contribution in Q3, but I think the real boost will be in Q4 in terms of the few thousand tests for the full year.

Dan Brennan, Analyst, TD Cowen: Great. Sorry, I think I don’t know if it’s my phone went in now, but thank you for that. And maybe if you can hear me, hopefully you can hear me okay. On price, so Kevin, obviously really strong price quarter. Would you be could you give us a sense of what the prior period collection was in the quarter, so we can kind of do our math?

Looks like you’re kind of guiding for the back half of the year somewhere between, call it 03/1950, like low 3600s in order to get to your exome genome revenue growth. Obviously, it’s a bit of a step down, but still super solid. Just wondering if you could help us think through what’s baked in and kind of the prior period impact this quarter.

Kevin Feeley, Chief Financial Officer, GeneDx: Yeah. So what’s if you look at pricing for the remainder of the year, you take the $37.18 we just posted in the second quarter, I think that’s a good number. Dan. And the reason I didn’t call out anything kind of unique or one off is that number, I think, is reflective of our cash collection experience in the second quarter and today, and should be relied upon. Now from guide perspective, the guide does absorb the ability as we enter into new indications or new call points to see a higher denial rate on the new stuff, if you will, and therefore, if you do the math on the guide anchored in achieving the 30% for the full year, which we remain convicted in, it does the guide allows for that rate to step down some in the back half of the year.

We have no particular reason to believe that that rate would step down other than the inherent nature of submitting things for the first time to payers on the new indications and new call points. The level of out of period adjustments have been fairly consistent over the past two years. The numbers disposed in the quarter, it ranges anywhere from like 3,000,000 to $6,000,000 but I think important to properly characterize the Q2 performance as really representative of the collection rate, and frankly, a function of the fact that we continue to reduce denials and improve collection.

Dan Brennan, Analyst, TD Cowen: I’m going to sneak one more in. Kathryn, you said in the prepared remarks, I think you said less than five percent of pediatricians already order for GP and IDD. So kind of you do the quick math, that’s like over 2,000 pediatricians, that’s where maybe your target early. Do you think you can begin to see some volume impact this year from those pediatricians? Just trying to solve for like what that early opportunity might look like.

Thank you.

Kathryn Stuhlen, President and Chief Executive Officer, GeneDx: Yeah, so we are going to be talking to pediatricians who are ordering from us today. But we don’t want to distract our team from ensuring that they are really focused on ped neuro and other specialists that are embedded into our plan. I would say contribution to this year from general pediatricians is gonna be very minimal. And I think we’ll start to see some more volumes in 2026 without a doubt. But I would say minimal for this year, because we do wanna make sure that the team continues to focus on the important growth opportunity that we have from the core.

Dan Brennan, Analyst, TD Cowen: Great. Okay, thank you.

Conference Operator: Thank you. One moment for the next question. And our next question is coming from the line of Subbu Nambi of Guggenheim. Your line is open.

Subbu Nambi, Analyst, Guggenheim: Hey, guys. Thank you for taking my question. Amazing quarter. A follow-up to Dave’s question. You are targeting 60,000 or so pediatricians.

First, how do you go about identifying pediatricians who have ordered genetic tests at some point? I know you’re going to use a targeted commercial approach where you’re going to learn before scaling up. What are the signs you’re looking for? What would make you expand quicker or slower?

Kathryn Stuhlen, President and Chief Executive Officer, GeneDx: Wonderful. So, just to zoom out to the general pediatrician opportunity, really, if you think about it, there are sixty thousand pediatricians in The US. About twenty five thousand of them see about six hundred thousand patients who have CDID. So, we think about that target group of pediatricians that we’ll first focus on as we start to enter the Gen T’s market, it would be the twenty five thousand who today are diagnosing patients with CDID. Of course, we want to see a day where all pediatricians are ordering the testing, but we think that from a segmentation standpoint, that 25,000 is the right area for us to focus on.

And so, as we think about the sales force, and planning to expand it as we enter into 2026, 25,000 will be the area that we really stay focused on in the beginning.

Conference Operator: Got it. Thank you for that,

Subbu Nambi, Analyst, Guggenheim: Catherine. This one’s for Kevin. The other panels were pretty strong compared to our estimate. What drove that strength? I thought you were deprioritizing targeted panel.

And then along those lines, how should we think about it in Q3 and Q4?

Kevin Feeley, Chief Financial Officer, GeneDx: Yeah, so you’re thinking about it correctly, that the sales team is not out there targeting and not incentivized, frankly, the past two years to bring in anything other than exome and genome. That said, as we activate new accounts, there are some non exome, non genome orders that come along for the ride with new doctors, which then tells us there’s an opportunity to educate physicians around the clinical benefits for exome and genome to continue our efforts to really move the industry away from individual gene tests and multi gene panels onto exome and genome. So the growth there, I would say, is nothing more than some success on activating new accounts, and gives us an opportunity to further educate those physicians now that they’re active owners of Gingyet. For the back half of the year, we tend to expect, since we’re not incentivizing the commercial team to grow that other panel line, so tend to expect flat or some slight attrition in that other panel line, with pickup in exome and genome, while at the same time, I’d say as we move further down the road to pediatricians, we’ll have to learn some of the initial experience to see if we see an increase in CMA, chromosome microarray orders, as we first start to approach pediatricians, but none of that expected to impact volumes in the second half of the year in a meaningful way.

Subbu Nambi, Analyst, Guggenheim: And, Kevin, just to be clear, you’re doing all of this passively, not incentivizing, but you’re taking in orders when it comes.

Dan Brennan, Analyst, TD Cowen: Correct.

Subbu Nambi, Analyst, Guggenheim: Got it. And last one from you guys. During the last quarter, you you mentioned that there’s a waiting room of clients for Epicora. And did you make meaningful steps to onboard all those clients? And is there still backlog, so to speak, of systems waiting to integrate?

Kathryn Stuhlen, President and Chief Executive Officer, GeneDx: Yeah, we absolutely have made progress. So, as I said, we have three that are live, and we’re continuing to bring more Epic Aura sites on, and we continue to build the pipeline there. So, we’re really pleased with how that business is continuing to shape up. And as I said, we’re contemplating that the fourth quarter will see the impact of those Epic aura implementations in a more meaningful way than in Q3. But we’re pleased to see volumes coming through when we’re bringing on Epic aura sites.

Conference Operator: Perfect. Thank you so much, guys. Thank you. One moment for the next question. And our next question will be coming from the line of William Bonello of Craig Hallum.

Your line is open.

Analyst: Hey, guys. Thanks for taking the questions. Couple of things. Kevin, I know you don’t give quarterly guidance, but given the commentary about a lot of the impact, at least on the NICU side really being more Q4 than Q3 and in the hopes to avoid a repeat of Q1. Can you give us any kind of sense of how you think volume growth might shake out between the third and the fourth quarter?

Kevin Feeley, Chief Financial Officer, GeneDx: Yeah. Hey, Bill. Look, the guide is anchored on our conviction today to deliver that 30% or more volume growth for the full year. So if you take last year’s test count at 30% or more, that gets you to about 96,900 tests. If were to back out what we just resulted in the first half of the year, that leaves roughly 53,200 in the back half of the year.

There is a seasonal dynamic that I’ll remind everybody about, with Q4 invariably being the strongest of any quarter throughout the year, Q1 the lightest of any quarter during the year, and Q3 does have some summer calendar effects to it. But we sit here today reaffirming that 30% full year year over year guide because of our conviction in it. So you might expect the second half of tests to kind of fall out with about 54% of that back half number in the fourth quarter.

Analyst: Okay, that’s really helpful. And then just on that number, and I know you addressed this a little response to Dan’s question, but I mean, it still is a really big ramp that’s implied in the back half of the year. And I guess, if it’s based on Catherine’s comments about maybe a few thousand NICU tests, that really quite get you there. So maybe just give us a little reason, a little bit more color on your level of confidence and why you feel so confident that either the new indications are really going to be kicking in or you’re seeing an acceleration the growth from the pediatric neurologists or allow us to believe that that ramp’s going to happen.

Kevin Feeley, Chief Financial Officer, GeneDx: Yeah, the majority of the second half ramp coming from outpatients, although that’s not to understate the long term importance of the NICU or our confidence to win that market. But if you look at the second half of the year, some of that confidence comes in the acceleration of growth we’ve now had in the second quarter, right? First quarter was 24 year over year, second quarter 28%. In order to get to the full year guide of 30% or more, the 30% mark would infer about 33% in the second half of the year, and has available to it a lot of levers that the first half didn’t, which includes some more time for new indications like cerebral palsy and others that we’ll be launching into to mature in terms of ramp from existing docs and new account activation. The first half didn’t have available to it any impact from pediatric immunologists that will begin to see an inflection in the second half of the year.

And we continue to see a growing increase in same store sales, as I called out, so a nice signal we saw in the second quarter was some of the talking points around new indications and a broader focus on education for physicians, we think, is making us more attractive to new accounts, but also just giving us a great reason to get back into the doctor’s office to reeducate them on the benefits of exome and genome first, and with a broader set of indications to talk about, we’re seeing signs that that’s gonna help increase same store sales.

Analyst: That’s really helpful. Thanks a lot. That’s all I had.

Conference Operator: Thank you. One moment for the next question. And our next question will be coming from the line of Mark Massario of BTIG. Your line is open.

Mark Massario, Analyst, BTIG: Hey, guys. Congratulations for a very nice quarter. I know in ’4, I believe your payment or denial rates were somewhere in the 50% range. And then I think in Q1, I believe you made some improvements. Your denial rate, I think, was somewhere around the high 40s or so.

Kevin, you talked about improvements management, so I would just be curious where you’re at today with the denial rate or the pay rate percentage.

Kevin Feeley, Chief Financial Officer, GeneDx: Yeah, the paid rate’s now and you’re tracking correctly, Mark, so thanks, the paid rate is now mid-50s, so a nice step up of a couple 100 basis points this quarter over last, and I think we remain convicted that there’s still a lot of room to run to reduce denials over time. Like I said, the guide assumes that on the portion of volume coming from new indications or new call points, there’s just an inherent nature, and therefore we’ve left some conservative room in the guide, but as we sit here today, the team is more well armed to have that back and forth boxing match with payers than we’ve ever been. So yeah, but I think you’re tracking correctly, and appreciate it.

Mark Massario, Analyst, BTIG: Awesome. I know, I think you guys have touched on this, but there were some inbounds this morning about the rationale to increase the Exome Genome revenue guide, to hold the Exome Genome volume guide. I’m pretty sure it has a lot to do with the success with the higher ASPs on exome genome, but can you maybe just fill that rationale out a little

Kevin Feeley, Chief Financial Officer, GeneDx: bit further just for folks? Yeah, think it reflects our best estimate of how the year is going to play out. Obviously, we’re very pleased with the performance in reimbursement rates. We think those rates are durable, and we’ll expect to see them rise, and so felt it’s important to reflect our confidence in the overall reimbursement dynamic to raise the revenue number, while at the same time, our outlook for the year has been and remains today even more confident in that 30% or higher volume mark, which is why we reaffirmed that.

Mark Massario, Analyst, BTIG: Awesome. And if I can sneak one more in, I’d be curious if you guys could expand a little bit more about how the Fabric Genomics is tracking relative to your expectations. I know that there were some customers that Fabric had that you guys may not have had. So I’d just be curious how that’s going and to what extent can that expand some of your opportunities.

Kathryn Stuhlen, President and Chief Executive Officer, GeneDx: Yeah, Fabric, we’re really happy that we acquired it. So, just out of the gate, it’s a fantastic team. Our team has begun really mapping out what integration looks like from porting our data into Fabric in order to ensure that we can really drive better diagnoses in a decentralized way, putting our data to work for more patients, as well as how do we think about the best of Fabrik, the best of GeneDx, and our ability to really put the strongest AI features into our interpretation capability. So, we’re excited about it. They’re on track with our plan this year in terms of their revenues, their gross margins.

The teams have had a fantastic time collaborating and really starting to work together. So, we’re excited about it. And again, as we think about the potential for where fabric can really help us drive the business. We’ve begun hiring sales reps for the international opportunity. So, we’re excited about the potential to start driving utilization of fabric via GeneDx in international markets.

It’s also a really important asset as we think about how to solve newborn screening, and ensure that patients have standardized results, whether a baby is born in London, or in Los Angeles. So, we’re really excited about the future potential within the capabilities of GeneDx. It’s off to a great start.

Mark Massario, Analyst, BTIG: It’s great to hear. Thanks, guys.

Conference Operator: Thank you. One moment for the next question. The next question will be coming from the line of Brandon Couillard of Wells Fargo. Your line is open.

Brandon Couillard, Analyst, Wells Fargo: Hey guys, thanks. Good morning. Kevin, do you think the second quarter volume growth benefited from any catch up benefit from the after the weather related disruptions you encountered in the first quarter at all?

Kevin Feeley, Chief Financial Officer, GeneDx: Yeah, think in the first quarter we said weather might have impacted Q1 one to two days, let’s call that 400 or 500 tests, and we also said at that time, missed appointments due to weather events in our space are not typically lost, but just deferred, and sometimes deferred for weeks or even months, And we saw that play out as expected. So yes, equal to the one or two days we called out as weather in Q1 and carried over to Q2, and then we saw a nice, good growth on top of that.

Brandon Couillard, Analyst, Wells Fargo: Okay. And then how much of the sequential OpEx growth came from the fabric deal as opposed to kind of organic investments? And how are we thinking about OpEx in the second half?

Kevin Feeley, Chief Financial Officer, GeneDx: Fabric was about $1,000,000 of OpEx in the quarter. That’s a partial quarter. We’ve owned the asset for two months in the second quarter. Look, as I said in my prepared remarks, certainly where we see opportunities to invest, to seize a leadership position in all these new markets, we will make those investments. I think at the same time, we want to signal that we think we have ample room for the business to drive leverage such that we can make substantial investments to dominate these markets while still driving a profitable business.

We think that’s important to do in the long run for shareholders, and we thought it important to call that out.

Brandon Couillard, Analyst, Wells Fargo: Great. Last one, Kathryn. The data business picked up a little bit in terms of revenue. Anything to watch out for on the pharma partnership front? Any milestones to look forward to later this year?

Thank you.

Kathryn Stuhlen, President and Chief Executive Officer, GeneDx: Certainly. So, think that business is healthy. We’re really happy to see same store sales there, both in terms of patient matching and in terms of people interested in GeneDx Discover, which is our data visualization product. So, we’re bringing on new customers. We’re continuing to sign more contracts within existing customers, and I expect we’ll continue to print and repeat that throughout the course of this year.

We remain we remain really optimistic about the future ability for us to put data to work in a much more meaningful way. And we’re starting to turn our attention to what that can look like in the future in terms of much broader collaborations with pharma companies. But today, we’re happy with the way that that business continues to perform, and we remain really optimistic about the potential for it in the future.

Brandon Couillard, Analyst, Wells Fargo: Great. Thanks.

Conference Operator: Thank you. And our next question will be coming from the line of Tycho Peterson of Jefferies. Your line is open.

Sabrina Dunbar, Investor Relations, GeneDx0: Hey, thanks. I appreciate all the color you guys have given on the AAP guidelines. Just one question we’ve gotten is just on the reliance on geneticists, you know, readiness to interpret reports, pediatricians are spread thin, workload, etcetera. Maybe just talk a little bit about the role you think they might play and to what degree that could be a rate limiting factor for adoption.

Kathryn Stuhlen, President and Chief Executive Officer, GeneDx: Yeah, that is a fantastic question, Tycho. So a couple of things. Pediatricians, their time is indeed tight. I think they have on average about twelve minutes per patient. We need to really make it easier for one of those clinicians to have access to testing.

So, when we talk about our customer experience, making it a best in class customer experience, it includes simplifying the entire ordering process on the front end, as well as on the back end, how do we simplify the report to make it easier for them to understand so they’re not reliant on a genetic counselor or a genetic expert? So how do we simplify the report? How do we make the care plans really easy to understand as well. So part of our customer experience that our product team is building out really, I would say, streamlines and simplifies that entire experience. So they’re not needing to be beholden to a genetic counselor or another genetics expert.

And part of that includes taking the knowledge base of genetic counselors and ensuring that whether it is through cat capabilities or otherwise throughout that entire customer experience that we can really scale the knowledge base that is currently existing within only about 2,000 genetic counselors that are out there. So, we think that customer experience challenge and opportunity is real, and we’re really excited about building that out. Importantly, is also how do we take some of the workload off of the pediatrician and empower parents? So how much of the parent portal can we build to make it easier and even more informed by a parent who’s super motivated to make sure that their child gets an answer. So, there’s really kind of this nice push and pull between how we simplify the ordering and report and customer service experience for the pediatrician, but also how do we engage with parents in a really smart way to offload some of the work from the pediatrician as well.

So, that is really an important part of what our team has started building. And we expect that we’ll start to see some of those features in 2026 that we think will help unlock the market.

Sabrina Dunbar, Investor Relations, GeneDx0: Okay, that’s helpful. And then maybe just following up on the pediatric market, just commercial payers, how do you think about the timeline to really get them on board? What’s needed to operationalize? Obviously, guidelines put a lot of pressure on them to come on board, but what how do you think about the timelines?

Kevin Feeley, Chief Financial Officer, GeneDx: Yeah. You’re right. Guidelines do put a lot of pressure. They don’t guarantee, but it certainly is an important tool that we will use to make the case to payers. Look, as we outlined, that eighteen to twenty four months from the time point between guidelines and inflection in terms of pull through is to build the product features.

Kathryn just talked about it’s to educate physicians, get them aware of the benefits and the guidelines, frankly. There’s a lot of buy side analysts who probably follow AAP guidelines more closely than pediatricians, so there is education for us to do, while at the same time, that gives us the lead time to build the dossier to approach payers to ensure they’re up to date with the latest literature, with the latest clinical and economic data, to show that the use of these tests frontline not only alleviates suffering and gives better insights to physicians, but can help avoid unnecessary costs for the health system and for insurers. And so rest assured, we’ll be making that case in earnest and and are already getting started on that.

Sabrina Dunbar, Investor Relations, GeneDx0: Okay. Last one. You know, as you kinda lap, you know, some of the biomarker bills that got added over the last twelve months, what should we we be watching on kind of the state front for the back half of the year? And then on Medicaid, have you sized the potential headwinds from the big beautiful bill cuts that were laid out?

Kathryn Stuhlen, President and Chief Executive Officer, GeneDx: So, were pleased to see additional states come on this past quarter, and so we’re now up to 35 in the outpatient, 17 in the inpatient, and we’ve expanded our government affairs team on the state side of things. So, we’re full court press in terms of continuing to drive the statewide. On HR1, I think the reality is not a material impact directly on our business. But, of course, any changes in Medicaid impacts every hospital system. I think what is beneficial for us is the health economic data that we have generated and that our field continues to generate that ensures that we’re actually making the healthcare system and every dollar that is allocated towards it go further.

We’re making the healthcare system more efficient. Going back to that pediatrician opportunity and the NICU opportunity, the five years on average that a child is undiagnosed is costing the healthcare system a lot of money today. And getting an answer as early as possible is going to save the healthcare system dollars. So, the health economic data that we are putting in front of Medicaid, in front of payers, in front of health systems, in front of policymakers is part of what is making the GeneDx opportunity one that is beneficial both from a clinical care perspective, but also in terms of the overall health care spend in this country. We think that there’s only strength ahead in terms of our ability to both impact in effect, change for the better for these kids, get an earlier diagnosis, and save everyone money along the way.

Sabrina Dunbar, Investor Relations, GeneDx0: And in terms of

Kevin Feeley, Chief Financial Officer, GeneDx: the state, Tycho, as Kathryn said, look, we picked up two new states with outpatient coverage despite some of the headline noise out there. I think a strong signal. Go back a year, there were 28 states, and we’re now up to 35 covering the test outpatient, so significant progress. In terms of what that number will be a year from now, it’s hard to tell. A lot of factors outside of our control.

From a guide perspective, we don’t count on any new states picking up coverage, and we take those as they come, but certainly the momentum is there.

Sabrina Dunbar, Investor Relations, GeneDx0: Okay, thank you.

Conference Operator: Thank you, and that does conclude today’s Q and A session. I would like to go ahead and turn the call back over to Kathy Sutle for closing remarks. Please go ahead.

Kathryn Stuhlen, President and Chief Executive Officer, GeneDx: Thank you all for your questions and for joining our call today. As we look ahead, we remain focused on execution, innovation, and expanding access to genomic insights that can truly transform care. Thank you for your continued support and belief in our vision. We look forward to updating you on our continued momentum next quarter.

Conference Operator: This does conclude today’s conference call. You may all disconnect.

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